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Aqueous micro and nanoreactors based on alternating copolymers of phenylmaleimide and vinylpyrrolidone bearing pendant l-proline stabilized with PEG grafted chains

机译:基于苯基马来酰亚胺和乙烯基吡咯烷酮的交替共聚物的水性微型和纳米反应器,该共聚物带有PEG接枝链稳定的L-脯氨酸侧基

摘要

Proline may work efficiently in water as catalyst of aldol reactions if it is hydrophobically activated. In this work, we have maximized this hydrophobic activation by the preparation of linear alternating copolymers of hydrophobic phenylmaleimide and a vinylpyrrolidone derivative bearing proline. These copolymers were water soluble above pH 5.0 and, unlike the free proline, exhibited efficient catalysis at pH 7.0. Moreover, they catalyzed and presented enantioselectivity in an aggregated form at pH 4.0 (close to the isoelectric point, IEP, of the polymer). This enantioselectivity has been related to the exclusion of water at this IEP. To control the size and stabilize the aggregates, PEG grafted copolymers were prepared by the incorporation of a PEG-macromer (2–10 mol%), which rendered stable nano-aggregates in water at the IEP. At this pH they catalyzed the aldol reaction in a higher rate than the non-grafted polymer, but the enantioselectivity was decreased. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016, 55, 1228–1236.
机译:如果脯氨酸被疏水活化,它可以在水中作为醛醇缩合反应的催化剂有效地起作用。在这项工作中,我们通过制备疏水性苯基马来酰亚胺和带有脯氨酸的乙烯基吡咯烷酮衍生物的线性交替共聚物来最大程度地提高了疏水性。这些共聚物在pH 5.0以上是水溶性的,并且与游离脯氨酸不同,在pH 7.0下显示出有效的催化作用。此外,它们在pH 4.0(接近聚合物的等电点,IEP)下以聚集形式催化并呈对映选择性。该对映选择性与该IEP中水的排除有关。为了控制尺寸并稳定聚集体,通过掺入PEG-macromer(2-10 mol%)制备了PEG接枝共聚物,该聚合物在IEP水中具有稳定的纳米聚集体。在此pH下,它们以比未接枝聚合物更高的速率催化羟醛反应,但对映选择性降低。 ©2016 Wiley Periodicals,Inc. J. Polym。科学,A部分:Polym。化学2016,55,1228–1236。

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